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The procedure accurately measures 5-alpha-dihydrotestosterone in blood, useful for standard tests.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

16-MHA can restore the barrier and moisture of damaged hair, making it similar to undamaged hair.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

A new method accurately measures lead levels in hair to assess exposure.

Keratin heterodimers are preferred for their specific and structural advantages.

HoxC genes are crucial for normal hair and nail development.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Dkk4 protein helps control how hair grows and its arrangement.

Dkk4 is necessary for the initial development and arrangement of hair follicles.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Lack of vitamin D receptor increases skin tumor risk by boosting hedgehog signaling.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

Analyzing isotopes from different tissues can effectively reveal detailed life histories of individuals.

Activating Wnt in skin cells controls the number of hair follicles by directing cell movement and fate.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Wnt and SHH signals together influence hair follicle cell development, offering insights for hair loss treatment.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Scientists discovered two versions of a new human hair keratin gene.

TCDD reduces EGF receptors in the liver, affecting growth and development.

Trichohyalin and peptidylarginine deiminase type III are found together in rat hair follicles, with trichohyalin being modified after expression.

Deuterium oxide extends the hair cycle duration in mice without changing hair structure.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Mutations in the DSG4 gene cause specific hair and scalp issues.

HHV-6 reactivation may be linked to psychiatric disorders and can improve with antiviral treatment.